Event Group
Event Groups are part of the Adverse Events Module within the Results Section. They provide a way to organize and summarize adverse event data by grouping related events together.
Each Event Group typically represents a category or class of adverse events and includes statistical information such as the number of participants affected and at risk for different event types: deaths, serious events, and other events.
Event Group path is as follows:
Study -> Results Section -> Adverse Events Module -> Event Group
Event Group
Ignite Creation Date:
2025-12-24 @ 5:03 PM
Ignite Modification Date:
2025-12-25 @ 2:42 PM
NCT ID:
NCT02497950
Group ID:
EG000
Title:
ELEVATE Patients
Description:
The ELEVATE study included 540 subjects of which: 463 pts received HM3 as primary implant and 19 pts received the HM3 as a replacement of another durable LVAD. These 2 groups ( 482 pts) consist the main study population, for which complete information has been collected. In addition, 58 patients had an outcome prior to having the possibility to sign the Informed Consent. For those, no patient data was collected, only duration of support and type of outcome (limited information available)
Deaths Number Affected:
209
Deaths Number At Risk:
None
Serious Number Affected:
407
Serious Number At Risk:
482
Other Number Affected:
277
Other Number At Risk:
482
Study:
NCT02497950
Results Section:
NCT02497950
Adverse Events Module:
NCT02497950